Zinc-finger protein ZFP318 is essential for expression of IgD, the alternatively spliced Igh product made by mature B lymphocytes

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 111; no. 12; pp. 4513 - 4518
• Main Authors: Enders, Anslem, Short, Alanna, Miosge, Lisa A., Bergmann, Hannes, Sontani, Yovina, Bertram, Edward M., Whittle, Belinda, Balakishnan, Bhavani, Yoshida, Kaoru, Sjollema, Geoff, Field, Matthew A., Andrews, T. Daniel, Hagiwara, Hiromi, Goodnow, Christopher C.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 25-03-2014; National Acad Sciences
• Subjects: Alternative Splicing; Amino Acid Sequence; Animals; B lymphocytes; B-Lymphocytes - metabolism; Biological Sciences; Bone marrow; Exons; Gene expression; Humans; Immatures; Immunoglobulin D - genetics; Immunoglobulin Heavy Chains - genetics; Immunoglobulins; Immunology; Lymphocytes; Messenger RNA; Mice; Molecular Sequence Data; Mutation; Mutation, Missense; Protein isoforms; Sequence Homology, Amino Acid; Spleen; Splicing; Zinc; Zinc Fingers; IgHd; IgHm; immunoglobulin isotype; ENU mutation
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1402739111

IgD and Igm are produced by alternative splicing of long primary RNA transcripts from the Ig heavy chain (Igh) locus and serve as the receptors for antigen on naïve mature B lymphocytes. IgM is made selectively in immature B cells, whereas IgD is coexpressed with IgM when the cells mature into follicular or marginal zone B cells, but the transacting factors responsible for this regulated change in splicing have remained elusive. Here, we use a genetic screen in mice to identify ZFP318, a nuclear protein with two U1-type zinc fingers found in RNA-binding proteins and no known role in the immune system, as a critical factor for IgD expression. A point mutation in an evolutionarily conserved lysine-rich domain encoded by the alternatively spliced Zfp318 exon 10 abolished IgD expression on marginal zone B cells, decreased IgD on follicular B cells, and increased IgM, but only slightly decreased the percentage of B cells and did not decrease expression of other maturation markers CD21, CD23, or CD62L. A targeted Zfp318 null allele extinguished IgD expression on mature B cells and increased IgM. Zfp318 mRNA is developmentally regulated in parallel with IgD, with little in pro-B cells, moderate amounts in immature B cells, and high levels selectively in mature follicular B cells. These findings identify ZFP318 as a crucial factor regulating the expression of the two major antibody isotypes on the surface of most mature B cells.